CY1110986T1 - AZOLIA AS INHIBITORS OF MILONYL-COZENZYME DISCARLIFICATION A USEFUL AS METABOLIC MODELS - Google Patents
AZOLIA AS INHIBITORS OF MILONYL-COZENZYME DISCARLIFICATION A USEFUL AS METABOLIC MODELSInfo
- Publication number
- CY1110986T1 CY1110986T1 CY20101101152T CY101101152T CY1110986T1 CY 1110986 T1 CY1110986 T1 CY 1110986T1 CY 20101101152 T CY20101101152 T CY 20101101152T CY 101101152 T CY101101152 T CY 101101152T CY 1110986 T1 CY1110986 T1 CY 1110986T1
- Authority
- CY
- Cyprus
- Prior art keywords
- useful
- milonyl
- discarlification
- cozenzyme
- azolia
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
- 230000002503 metabolic effect Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- RGJOEKWQDUBAIZ-IBOSZNHHSA-N CoASH Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCS)O[C@H]1N1C2=NC=NC(N)=C2N=C1 RGJOEKWQDUBAIZ-IBOSZNHHSA-N 0.000 abstract 2
- 208000010444 Acidosis Diseases 0.000 abstract 1
- 208000024172 Cardiovascular disease Diseases 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 208000008589 Obesity Diseases 0.000 abstract 1
- 230000007950 acidosis Effects 0.000 abstract 1
- 208000026545 acidosis disease Diseases 0.000 abstract 1
- RGJOEKWQDUBAIZ-UHFFFAOYSA-N coenzime A Natural products OC1C(OP(O)(O)=O)C(COP(O)(=O)OP(O)(=O)OCC(C)(C)C(O)C(=O)NCCC(=O)NCCS)OC1N1C2=NC=NC(N)=C2N=C1 RGJOEKWQDUBAIZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005516 coenzyme A Substances 0.000 abstract 1
- 229940093530 coenzyme a Drugs 0.000 abstract 1
- KDTSHFARGAKYJN-UHFFFAOYSA-N dephosphocoenzyme A Natural products OC1C(O)C(COP(O)(=O)OP(O)(=O)OCC(C)(C)C(O)C(=O)NCCC(=O)NCCS)OC1N1C2=NC=NC(N)=C2N=C1 KDTSHFARGAKYJN-UHFFFAOYSA-N 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 208000030159 metabolic disease Diseases 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 235000020824 obesity Nutrition 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/423—Oxazoles condensed with carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/426—1,3-Thiazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/428—Thiazoles condensed with carbocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/541—Non-condensed thiazines containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Η παρούσα εφεύρεση αναφέρεται σε μεθόδους θεραπευτικής αγωγής ορισμένων μεταβολικών νοσημάτων, και σε νέες ενώσεις και σε προφάρμακα, ή/και φαρμακευτικώς αποδεκτά άλατα αυτών, σε φαρμακευτικές συνθέσεις που περιέχουν τέτοιες ενώσεις χρήσιμες στη θεραπεία τέτοιων νοσημάτων. Συγκεκριμένα, η παρούσα εφεύρεση αναφέρεται στη χρησιμοποίηση νέων ενώσεων και συνθέσεων για τη θεραπευτική αγωγή καρδιαγγειακών νοσημάτων, διαβήτη, καρκίνων, οξέωσης, και παχυσαρκίας μέσω της αναστολής της αποκαρβοξυλάσης μηλονυλο-συνενζύμου A (MCD). Αυτές οι ενώσεις έχουν τους τύπους (I) και (II), όπου τα Υ, C, R1, R2, R6 και R7 ορίζονται στην παρούσα.The present invention relates to methods of treating certain metabolic diseases, and to novel compounds and prodrugs, and / or pharmaceutically acceptable salts thereof, to pharmaceutical compositions containing such compounds useful in the treatment of such diseases. In particular, the present invention relates to the use of novel compounds and compositions for the treatment of cardiovascular disease, diabetes, cancers, acidosis, and obesity by inhibiting malolyl coenzyme A (MCD) decarboxylase. These compounds have the formulas (I) and (II), wherein Y, C, R1, R2, R6 and R7 are defined herein.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US27003401P | 2001-02-20 | 2001-02-20 | |
EP02721032A EP1370260B1 (en) | 2001-02-20 | 2002-02-19 | Azoles as malonyl-coa decarboxylase inhibitors useful as metabolic modulators |
Publications (1)
Publication Number | Publication Date |
---|---|
CY1110986T1 true CY1110986T1 (en) | 2015-06-11 |
Family
ID=23029607
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CY20101101152T CY1110986T1 (en) | 2001-02-20 | 2010-12-14 | AZOLIA AS INHIBITORS OF MILONYL-COZENZYME DISCARLIFICATION A USEFUL AS METABOLIC MODELS |
Country Status (24)
Country | Link |
---|---|
US (1) | US7723366B2 (en) |
EP (2) | EP1379243B1 (en) |
JP (4) | JP4159361B2 (en) |
KR (1) | KR100659427B1 (en) |
CN (1) | CN100383132C (en) |
AT (2) | ATE442141T1 (en) |
AU (1) | AU2002251987B2 (en) |
BR (1) | BR0207408A (en) |
CA (1) | CA2437409C (en) |
CY (1) | CY1110986T1 (en) |
DE (2) | DE60233650D1 (en) |
DK (1) | DK1370260T3 (en) |
ES (2) | ES2330417T3 (en) |
HK (1) | HK1062633A1 (en) |
HU (1) | HU229431B1 (en) |
IL (2) | IL156827A0 (en) |
MX (1) | MXPA03007441A (en) |
NO (1) | NO20033665L (en) |
NZ (1) | NZ526883A (en) |
PL (1) | PL204456B1 (en) |
PT (1) | PT1370260E (en) |
RU (1) | RU2258706C2 (en) |
SI (1) | SI1370260T1 (en) |
WO (2) | WO2002066035A2 (en) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7709510B2 (en) * | 2001-02-20 | 2010-05-04 | Chugai Seiyaku Kabushiki Kaisha | Azoles as malonyl-CoA decarboxylase inhibitors useful as metabolic modulators |
PL204456B1 (en) * | 2001-02-20 | 2010-01-29 | Chugai Pharmaceutical Co Ltd | Azoles as malonyl-coa decarboxylase inhibitors useful as metabolic modulators |
WO2003090746A1 (en) * | 2002-04-23 | 2003-11-06 | Chugai Seiyaku Kabushiki Kaisha | 1,3-thiazoles as lxr modulators in the treatment of cardiovascular diseases |
ES2295930T3 (en) * | 2003-08-01 | 2008-04-16 | Chugai Seiyaku Kabushiki Kaisha | CIANOAMIDE COMPOUNDS USED AS MALONIL-COA DESCARBOXYLASE INHIBITORS. |
EP1658071B1 (en) * | 2003-08-01 | 2008-09-10 | Chugai Seiyaku Kabushiki Kaisha | Cyanoguanidine-based azole compounds useful as malonyl-coa decarboxylase inhibitors |
JP4648317B2 (en) * | 2003-08-01 | 2011-03-09 | 中外製薬株式会社 | Piperidine compounds useful as malonyl-CoA decarboxylase inhibitors |
EP1653944B1 (en) | 2003-08-01 | 2010-11-10 | Chugai Seiyaku Kabushiki Kaisha | Heterocyclic compounds useful as malonyl-coa decarboxylase inhibitors |
AU2005261740A1 (en) * | 2004-07-08 | 2006-01-19 | Novo Nordisk A/S | Polypeptide protracting tags comprising a tetrazole moiety |
AU2007326395B2 (en) * | 2006-12-01 | 2012-10-11 | Msd K.K. | Novel phenyl-isoxazol-3-ol derivative |
US20110065739A1 (en) * | 2008-06-02 | 2011-03-17 | Makoto Ishikawa | Novel isoxazole drivative |
CA2796459C (en) | 2010-04-16 | 2016-05-24 | Salk Institute For Biological Studies | Methods for treating metabolic disorders using fgf-1 |
SG11201603134XA (en) * | 2013-10-21 | 2016-05-30 | Salk Inst For Biological Studi | Mutated fibroblast growth factor (fgf) 1 and methods of use |
WO2015061331A1 (en) | 2013-10-21 | 2015-04-30 | Salk Institute For Biological Studies | Chimeric fibroblast growth factor (fgf) 2/fgf1 peptides and methods of use |
CA3002400A1 (en) | 2015-10-30 | 2017-05-04 | Salk Institute For Biological Studies | Treatment of steroid-induced hyperglycemia with fibroblast growth factor (fgf) 1 analogs |
JOP20190024A1 (en) | 2016-08-26 | 2019-02-19 | Gilead Sciences Inc | Substituted pyrrolizine compounds and uses thereof |
CN117100751A (en) | 2017-06-20 | 2023-11-24 | 安布里亚制药公司 | Compositions and methods for improving cardiac metabolic efficiency |
US10836769B2 (en) | 2018-02-26 | 2020-11-17 | Gilead Sciences, Inc. | Substituted pyrrolizine compounds and uses thereof |
EP3866794A4 (en) | 2018-10-17 | 2022-07-20 | Imbria Pharmaceuticals, Inc. | Methods of treating rheumatic diseases using trimetazidine-based compounds |
US11542309B2 (en) | 2019-07-31 | 2023-01-03 | Salk Institute For Biological Studies | Fibroblast growth factor 1 (FGF1) mutant proteins that selectively activate FGFR1B to reduce blood glucose |
US11530184B2 (en) | 2020-06-30 | 2022-12-20 | Imbria Pharmaceuticals, Inc. | Crystal forms of 2-[4-[(2,3,4-trimethoxyphenyl)methyl]piperazin-1-yl]ethyl pyridine-3-carboxylate |
US11780811B2 (en) | 2020-06-30 | 2023-10-10 | Imbria Pharmaceuticals, Inc. | Methods of synthesizing 2-[4-[(2,3,4-trimethoxyphenyl)methyl]piperazin-1-yl]ethyl pyridine-3-carboxylate |
US11883396B2 (en) | 2021-05-03 | 2024-01-30 | Imbria Pharmaceuticals, Inc. | Methods of treating kidney conditions using modified forms of trimetazidine |
CN114767665B (en) * | 2021-06-11 | 2023-10-10 | 同济大学 | Use of 5-tetradecyloxy-2-furancarboxylic acid in preparation of medicament for treating psoriasis-like dermatitis |
Family Cites Families (91)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2863874A (en) | 1955-05-26 | 1958-12-09 | Goodrich Co B F | Process of preparing 2-aminothiazoles |
US3728455A (en) | 1971-06-24 | 1973-04-17 | American Cyanamid Co | Novel compositions of matter |
EP0144101B1 (en) | 1983-11-30 | 1991-02-06 | Janssen Pharmaceutica N.V. | Bicyclic heterocyclyl containing n-(bicyclic heterocyclyl)-4-piperidinamines |
JPS60202872A (en) | 1984-03-27 | 1985-10-14 | Kaken Pharmaceut Co Ltd | Benzofuran derivative, its preparation, and hypotensive agent containing said derivative as active component |
CA1281325C (en) | 1984-06-20 | 1991-03-12 | Patrice C. Belanger | Benzofuran derivatives |
US4783443A (en) | 1986-03-03 | 1988-11-08 | The University Of Chicago | Amino acyl cephalosporin derivatives |
GB8714537D0 (en) | 1987-06-22 | 1987-07-29 | Ici Plc | Pyrazine derivatives |
EP0733366B1 (en) | 1988-01-07 | 1998-04-01 | E.I. Du Pont De Nemours And Company | Pharmaceutical compositions comprising angiotensin II receptor blocking imidazoles and diuretics |
JP2568315B2 (en) | 1989-06-30 | 1997-01-08 | イー・アイ・デュポン・ドゥ・ヌムール・アンド・カンパニー | Fused ring aryl substituted imidazole |
EP0479903B1 (en) | 1989-06-30 | 1996-02-21 | E.I. Du Pont De Nemours And Company | Substituted imidazoles useful as angiotensin ii blockers |
SU1681502A1 (en) | 1989-07-26 | 1994-06-15 | Всесоюзный Научно-Исследовательский Химико-Фармацевтический Институт Им.С.Орджоникидзе | 3-(2, 5-dimethoxybenzoyl)-4-dimethylaminomethyl-5- hydroxy-6-bromobenzofuran hydrochloride showing analgetic, local anesthetic, anticonvulsant, antiarrythmic, stimulating coronary, cerebral and renal blood circulation effects |
RU1743153C (en) | 1990-06-04 | 1995-02-27 | ВНИИ химических средств защиты растений | N-[4-2'-(hydroxyhexafluoroisopropyl)phenyl]-n- ethyl-n'-phenylurea showing growth- regulating and antidote action |
ATE146076T1 (en) | 1990-06-22 | 1996-12-15 | Du Pont | TREATMENT OF CHRONIC KIDNEY FAILURE WITH IMIDAZOLE ANGIOTENSIN II RECEPTOR ANTAGONISTS |
CA2053216C (en) | 1990-10-12 | 2003-04-08 | Michel L. Belley | Saturated hydroxyalkylquinoline acids as leukotriene antagonists |
US5470975A (en) | 1990-10-16 | 1995-11-28 | E.R. Squibb & Sons, Inc. | Dihydropyrimidine derivatives |
CA2053148A1 (en) | 1990-10-16 | 1992-04-17 | Karnail Atwal | Dihydropyrimidine derivatives |
US5374615A (en) | 1990-10-31 | 1994-12-20 | E. R. Squibb & Sons, Inc. | Indole- and benzimidazole-substituted imidazole and benzimidazole derivatives |
SU1825496A3 (en) | 1991-04-04 | 1994-12-30 | Всесоюзный научно-исследовательский институт химических средств защиты растений | Derivatives of n-[4-(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)phenyl- ]urea showing antidote activity to 2-chloro-n-[(4-methoxy-6-methyl-1,3,5-triazine-2-yl)aminocarb- onyl]benzene sulfamide in flax sowing |
JPH05124925A (en) * | 1991-04-09 | 1993-05-21 | Sansho Seiyaku Co Ltd | External preparation with melanin production-inhibitory activity |
US5190942A (en) | 1991-04-22 | 1993-03-02 | E. R. Squibb & Sons, Inc. | Benzoxazole and related heterocyclic substituted imidazole and benzimidazole derivatives |
US5256695A (en) | 1991-07-24 | 1993-10-26 | E. R. Squibb & Sons, Inc. | Acyl amidine and acyl guanidine substituted biphenyl derivatives |
US5177097A (en) | 1991-07-24 | 1993-01-05 | E. R. Squibb & Sons, Inc. | Acyl amidine and acyl, guanidine substituted biphenyl derivatives |
CA2115990A1 (en) | 1991-08-19 | 1993-03-04 | George Albert Boswell | Angiotensin ii receptor blocking imidazolinone derivatives |
US5212177A (en) | 1991-12-16 | 1993-05-18 | E. R. Squibb & Sons, Inc. | Indole and benzimidazole-substituted dihydropyrimidine derivatives |
US5350752A (en) | 1991-12-16 | 1994-09-27 | E. R. Squibb & Sons, Inc. | Dihydropyrimidine derivatives |
US5225408A (en) | 1991-12-20 | 1993-07-06 | E. R. Squibb & Sons, Inc. | Biphenyl oxadiazinone angiotensin II inhibitors |
TW297025B (en) | 1992-02-14 | 1997-02-01 | Squibb & Sons Inc | |
US5208235A (en) | 1992-03-10 | 1993-05-04 | E. R. Squibb & Sons, Inc. | Indole- and benzimidazole-substituted imidazole derivatives |
US5208234A (en) | 1992-03-10 | 1993-05-04 | E. R. Squibb & Sons, Inc. | Substituted imidazole phosphonic and phosphinic acid derivatives |
WO1993021168A1 (en) | 1992-04-10 | 1993-10-28 | Merck Frosst Canada Inc. | Thiazole-substituted benzyl alcohols as leukotriene antagonists |
US5506227A (en) | 1992-04-13 | 1996-04-09 | Merck Frosst Canada, Inc. | Pyridine-substituted benzyl alcohols as leukotriene antagonists |
US5378704A (en) | 1992-04-15 | 1995-01-03 | E. R. Squibb & Sons, Inc. | Non-peptidic angiotensin-II-receptor-antagonists |
US5534347A (en) | 1992-09-04 | 1996-07-09 | Eastman Kodak Company | Fusing roll having a fluorocarbon-silicone barrier layer |
CA2147990C (en) | 1992-10-30 | 2001-02-20 | Keith D. Weiss | Low viscosity magnetorheological materials |
GB9226860D0 (en) | 1992-12-23 | 1993-02-17 | Leo Pharm Prod Ltd | Novel treatment |
EP0679157B1 (en) | 1993-01-15 | 1997-11-19 | G.D. Searle & Co. | Novel 3,4-diaryl thiophenes and analogs thereof having use as antiinflammatory agents |
DE4302681A1 (en) | 1993-02-01 | 1994-08-04 | Hoechst Ag | Sulfonic acid esters, radiation-sensitive mixtures produced therewith and their use |
DE4306152A1 (en) | 1993-02-27 | 1994-09-01 | Hoechst Ag | Positive-working radiation-sensitive mixture, and recording material produced therewith |
JPH07188227A (en) | 1993-12-24 | 1995-07-25 | Japan Tobacco Inc | Thiazolidine derivative and oxazole derivative |
JPH09509156A (en) | 1994-02-03 | 1997-09-16 | ケンブリッジ・ニューロサイエンス・インコーポレーテッド | Therapeutic guanidines |
US5519040A (en) | 1994-04-29 | 1996-05-21 | Allergan | Substituted thiazole sulfonamides as antiglaucoma agents |
JPH10503176A (en) | 1994-06-17 | 1998-03-24 | コーバス インターナショナル, インコーポレイテッド | 3-Amino-2-oxo-1-piperidineacetic acid derivatives as enzyme inhibitors |
US5932733A (en) | 1994-06-17 | 1999-08-03 | Corvas International, Inc. | 3-amino-2-oxo-1-piperidineacetic derivatives containing an arginine mimic as enzyme inhibitors |
US5637599A (en) | 1994-06-17 | 1997-06-10 | Corvas International, Inc. | Arginine mimic derivatives as enzyme inhibitors |
US5519143A (en) | 1994-09-19 | 1996-05-21 | The Du Pont Merck Pharmaceutical Company | Process for the isolation and purification of an imidazole stereoisomer from a mixture of stereoisomers by selective precipitation |
US5552437A (en) | 1994-10-27 | 1996-09-03 | Merck Frosst Canada, Inc. | Bisarylcarbinol derivatives as inhibitors of leukotriene biosynthesis |
US5527827A (en) | 1994-10-27 | 1996-06-18 | Merck Frosst Canada, Inc. | Bisarylcarbinol cinnamic acids as inhibitors of leukotriene biosynthesis |
US5674876A (en) | 1995-01-20 | 1997-10-07 | Research Development Foundation | ρ-heteroatom-substituted phenols and uses thereof |
JPH08311036A (en) | 1995-03-14 | 1996-11-26 | Takeda Chem Ind Ltd | Pyrazole derivative, its use |
IL117534A0 (en) | 1995-03-24 | 1996-07-23 | Rhone Poulenc Agrochimie | Reagent and process which are useful for grafting a substituted difluoromethyl group onto a compound containing at least one electrophilic function |
JPH0912585A (en) | 1995-06-30 | 1997-01-14 | Ube Ind Ltd | Highly coordinated typical element complex |
ATE203234T1 (en) | 1995-08-30 | 2001-08-15 | Searle & Co | META-GUANIDINE, UREA, THIOUREA OR AZACYCLIC AMINOBENZOIC ACID DERIVATIVES AS INTEGRIN ANTAGONISTS |
JPH09124632A (en) | 1995-10-31 | 1997-05-13 | Sankyo Co Ltd | Benzo-heterocyclic derivative |
FR2756825B1 (en) * | 1996-12-10 | 1999-01-08 | Adir | NOVEL [3H] -BENZOXAZOLE-2-THIONES AND [3H] - BENZOTHIAZOLE-2-THIONES DERIVATIVES, THEIR PREPARATION METHOD AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
GB2321244B (en) | 1997-01-20 | 2000-11-22 | Pharmacia & Upjohn Spa | Vitamin D3 analogues,process for preparing them,and their use as antiproliferative and antitumour agents |
DE19716231A1 (en) | 1997-04-18 | 1998-10-22 | Studiengesellschaft Kohle Mbh | Olefin metathesis in compressed carbon di:oxide |
DE19722952A1 (en) | 1997-05-31 | 1998-12-03 | Huels Chemische Werke Ag | Use of polymers comprising units of fluorine atom(s) on carbon atom |
US5895771A (en) | 1997-06-05 | 1999-04-20 | Akzo Nobel Nv | Fluorinated alkoxy and/or aryloxy aluminates as cocatalysts for metallocene-catalyzed olefin polymerizations |
US5977413A (en) | 1997-08-04 | 1999-11-02 | Nippon Kayaku Kabushiki Kaisha | Method for producing bis(3-amino-4-hydroxyphenyl) compounds |
WO1999012938A1 (en) | 1997-09-11 | 1999-03-18 | Colorado State University Research Foundation | Weakly coordinating anions containing polyfluoroalkoxide ligands |
WO1999047497A2 (en) | 1998-03-13 | 1999-09-23 | Merck Frosst Canada & Co. | Carboxylic acids and acylsulfonamides, compositions containing such compounds and methods of treatment |
GB2337701A (en) | 1998-05-26 | 1999-12-01 | United Medical And Dental Schools Of Guys St Thomas Hospitals | Treatment of ischemia with an angiotensin II antagonist |
DE19825182A1 (en) * | 1998-06-05 | 1999-12-09 | Agfa Gevaert Ag | Chemical sensitization of silver halide emulsion with high chloride content |
DE69923681T2 (en) | 1998-06-18 | 2006-01-12 | Bristol-Myers Squibb Co. | CARBON SUBSTITUTED AMINOTHIAZOLE AS INHIBITORS OF CYCLINE-DEPENDENT KINASES |
AU774628B2 (en) * | 1998-08-11 | 2004-07-01 | Governors Of The University Of Alberta, The | Compositions and methods for identifying mammalian malonyl coa decarboxylase inhibitors, agonists and antagonists |
FR2784114B1 (en) | 1998-09-18 | 2001-02-02 | Thomson Csf | POLYMERIC MATERIALS ABSORBING ORGANOPHOSPHORUS COMPOUNDS. PROCESS FOR THE SYNTHESIS OF THESE MATERIALS. CHEMICAL SENSORS COMPRISING SUCH MATERIALS |
ATE286923T1 (en) | 1998-10-05 | 2005-01-15 | Promerus Llc | CATALYST AND PROCESS FOR POLYMERIZING CYCLOOLEFINES |
JP2000128878A (en) | 1998-10-28 | 2000-05-09 | Teijin Ltd | Benzofuryl-alpha-pyridone derivative |
DE69925939T2 (en) | 1998-12-09 | 2006-05-04 | Sumitomo Bakelite Co. Ltd. | ADDITION POLYMERIZATION IN A FORM USING NORBORNE TYPE POLYMERS WITH GROUP 3 METAL COMPLEXES |
JP2002533318A (en) | 1998-12-22 | 2002-10-08 | ニューロサーチ、アクティーゼルスカブ | Ion channel regulator |
ES2315456T3 (en) | 1998-12-23 | 2009-04-01 | Smithkline Beecham Corporation | DERIVATIVES OF 4-AMINO-AZEPAN-3-ONA AS PROTEASA INHIBITORS. |
US20030144175A1 (en) | 1998-12-23 | 2003-07-31 | Smithkline Beecham Corporation | Protease inhibitors |
CA2362401A1 (en) | 1999-02-04 | 2000-08-10 | Paul Fleming | G-protein coupled heptahelical receptor binding compounds and methods of use thereof |
CA2360305A1 (en) | 1999-02-09 | 2000-08-17 | Bristol-Myers Squibb Company | Lactam inhibitors of fxa and method |
GB9904933D0 (en) | 1999-03-04 | 1999-04-28 | Glaxo Group Ltd | Compounds |
US6316503B1 (en) | 1999-03-15 | 2001-11-13 | Tularik Inc. | LXR modulators |
IL146006A0 (en) * | 1999-05-17 | 2002-07-25 | Novo Nordisk As | Glucagon antagonists/inverse agonists |
US6503949B1 (en) * | 1999-05-17 | 2003-01-07 | Noro Nordisk A/S | Glucagon antagonists/inverse agonists |
EP1212065A4 (en) | 1999-07-08 | 2004-02-11 | Tularik Inc | Compositions and methods for raising hdl cholesterol levels |
ATE289291T1 (en) | 1999-09-24 | 2005-03-15 | Ono Pharmaceutical Co | HYDROXAMIC ACID DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND MEDICATIONS WHICH CONTAIN THEM AS THE ACTIVE INGREDIENTS |
HUP0301231A2 (en) | 2000-06-14 | 2003-08-28 | Smithkline Beecham Corp. | Protease inhibitors, pharmaceutical compositions containing them and their use |
HU227197B1 (en) | 2000-10-24 | 2010-10-28 | Richter Gedeon Nyrt | Nmda receptor antagonist carboxylic acid amide derivatives and pharmaceutical compositions containing them |
CA2435067C (en) | 2001-01-26 | 2011-11-15 | Chugai Seiyaku Kabushiki Kaisha | Malonyl-coa decarboxylase inhibitors useful as metabolic modulators |
ATE341539T1 (en) | 2001-01-26 | 2006-10-15 | Chugai Pharmaceutical Co Ltd | MALONYL COA-DECARBOXYLASE INHIBITORS AS METABOLISM MODULATORS |
AU2002236830A1 (en) | 2001-01-26 | 2002-08-06 | Chugai Seiyaku Kabushiki Kaisha | Methods for the treatment of diseases using malonyl-coa decarbox ylase inhibitors |
PL204456B1 (en) | 2001-02-20 | 2010-01-29 | Chugai Pharmaceutical Co Ltd | Azoles as malonyl-coa decarboxylase inhibitors useful as metabolic modulators |
US7709510B2 (en) | 2001-02-20 | 2010-05-04 | Chugai Seiyaku Kabushiki Kaisha | Azoles as malonyl-CoA decarboxylase inhibitors useful as metabolic modulators |
EP1658071B1 (en) | 2003-08-01 | 2008-09-10 | Chugai Seiyaku Kabushiki Kaisha | Cyanoguanidine-based azole compounds useful as malonyl-coa decarboxylase inhibitors |
JP4648317B2 (en) | 2003-08-01 | 2011-03-09 | 中外製薬株式会社 | Piperidine compounds useful as malonyl-CoA decarboxylase inhibitors |
EP1653944B1 (en) | 2003-08-01 | 2010-11-10 | Chugai Seiyaku Kabushiki Kaisha | Heterocyclic compounds useful as malonyl-coa decarboxylase inhibitors |
ES2295930T3 (en) | 2003-08-01 | 2008-04-16 | Chugai Seiyaku Kabushiki Kaisha | CIANOAMIDE COMPOUNDS USED AS MALONIL-COA DESCARBOXYLASE INHIBITORS. |
-
2002
- 2002-02-19 PL PL362274A patent/PL204456B1/en not_active IP Right Cessation
- 2002-02-19 EP EP02742484A patent/EP1379243B1/en not_active Expired - Lifetime
- 2002-02-19 HU HU0303272A patent/HU229431B1/en not_active IP Right Cessation
- 2002-02-19 EP EP02721032A patent/EP1370260B1/en not_active Expired - Lifetime
- 2002-02-19 JP JP2002565592A patent/JP4159361B2/en not_active Expired - Fee Related
- 2002-02-19 DK DK02721032.7T patent/DK1370260T3/en active
- 2002-02-19 ES ES02742484T patent/ES2330417T3/en not_active Expired - Lifetime
- 2002-02-19 JP JP2002565593A patent/JP4155351B2/en not_active Expired - Fee Related
- 2002-02-19 KR KR1020037010409A patent/KR100659427B1/en not_active IP Right Cessation
- 2002-02-19 BR BR0207408-7A patent/BR0207408A/en not_active IP Right Cessation
- 2002-02-19 DE DE60233650T patent/DE60233650D1/en not_active Expired - Lifetime
- 2002-02-19 DE DE60238391T patent/DE60238391D1/en not_active Expired - Lifetime
- 2002-02-19 WO PCT/US2002/004777 patent/WO2002066035A2/en not_active Application Discontinuation
- 2002-02-19 CN CNB028052161A patent/CN100383132C/en not_active Expired - Fee Related
- 2002-02-19 SI SI200230929T patent/SI1370260T1/en unknown
- 2002-02-19 ES ES02721032T patent/ES2353686T3/en not_active Expired - Lifetime
- 2002-02-19 AT AT02742484T patent/ATE442141T1/en not_active IP Right Cessation
- 2002-02-19 MX MXPA03007441A patent/MXPA03007441A/en active IP Right Grant
- 2002-02-19 AU AU2002251987A patent/AU2002251987B2/en not_active Ceased
- 2002-02-19 US US10/468,378 patent/US7723366B2/en not_active Expired - Fee Related
- 2002-02-19 WO PCT/US2002/004729 patent/WO2002066034A1/en active Application Filing
- 2002-02-19 RU RU2003128307/04A patent/RU2258706C2/en not_active IP Right Cessation
- 2002-02-19 IL IL15682702A patent/IL156827A0/en unknown
- 2002-02-19 CA CA2437409A patent/CA2437409C/en not_active Expired - Fee Related
- 2002-02-19 AT AT02721032T patent/ATE489089T1/en active
- 2002-02-19 NZ NZ526883A patent/NZ526883A/en not_active IP Right Cessation
- 2002-02-19 PT PT02721032T patent/PT1370260E/en unknown
-
2003
- 2003-07-08 IL IL156827A patent/IL156827A/en not_active IP Right Cessation
- 2003-08-19 NO NO20033665A patent/NO20033665L/en not_active Application Discontinuation
-
2004
- 2004-06-16 HK HK04104396.8A patent/HK1062633A1/en not_active IP Right Cessation
-
2007
- 2007-12-10 JP JP2007318038A patent/JP4842247B2/en not_active Expired - Fee Related
- 2007-12-17 JP JP2007324412A patent/JP4879152B2/en not_active Expired - Fee Related
-
2010
- 2010-12-14 CY CY20101101152T patent/CY1110986T1/en unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CY1110986T1 (en) | AZOLIA AS INHIBITORS OF MILONYL-COZENZYME DISCARLIFICATION A USEFUL AS METABOLIC MODELS | |
NO2023022I1 (en) | cobimetinib, optionally in any form protected by the basic patent, including harmaceutically acceptable salts and sovates thereof, particularly cobimetinib hemifumarate | |
CY1121639T1 (en) | COMPOSITIONS CONTAINING NUCLEOTIDE AND OLIGONUCLEOTIDE PRODRUGS | |
CY1106674T1 (en) | AZADICYCLIC HETERCYCLES AS CANNABINOID RECEPTOR REGULATORS | |
CY1105047T1 (en) | PYRIDOPYRIMIDINONE COMPOUNDS, THEIR METHOD OF PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM | |
CY1107084T1 (en) | PYRROLOPYRIDAZINE PRODUCERS | |
TW200526658A (en) | Heterocyclic inhibitors of MEK and methods of use thereof | |
CY1109227T1 (en) | Derivative of 5-phenyl-4-methyl-thiazol-2-yl-amine as Inhibitors of the Phosphatidylinositol 3 (P13) Thionyl Methyl Enzyme (P13) Thionyl | |
CY1113766T1 (en) | INDOLIDONES PRODUCTS FOR THE TREATMENT OR PREVENTION OF DISEASES | |
CY1108292T1 (en) | DMXAA ANTI-CANCER CONTAINER | |
IS2833B (en) | ÉÅQ┴Bens├│├╛├¡├│sep├¡n┴og┴notkun┴├╛eirra┴gegn┴fitubl├Ó├░i┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴┴ | |
ATE369353T1 (en) | MEDICALLY USABLE ARYLETHANOLAMINE COMPOUNDS | |
EA201001669A1 (en) | SUBSTITUTED PYRIMIDIN-5-CARBOXAMIDES 281 | |
IS7965A (en) | Thienopyrimidinedione and their use in the development of self-hypersensitivity disease | |
IS2517B (en) | Use of substituted 2-aminotetralins in the prevention of Parkinson's disease | |
DK1519724T3 (en) | Fredericamycin derivatives as drugs for the treatment of tumors | |
DK1767535T3 (en) | Synthesis of epothilones, their intermediates, analogs and their use | |
CY1107985T1 (en) | CCR1 competitors for the treatment of other degenerative inflammatory diseases | |
EA200401114A2 (en) | SUBSTITUTED HYDROXYETHYLAMINES | |
EA200600223A1 (en) | SUBSTITUTED 2-AMINOTHETRALINES FOR THE TREATMENT OF DEPRESSION | |
DE602004008959D1 (en) | BENZOÄBÜÄ1,4ÜDIOXEPINDERIVATE | |
CY1110130T1 (en) | MORPHOLINE PRODUCTS FOR USE AS DOPAMINE AGONISTS IN THERAPEUTIC DISEASE Therapeutic Treatment I.A. | |
ATE409480T1 (en) | PYRAZOLOA3,4-BUPYRIDINE-6-ONE AS GSK-3 INHIBITORS | |
SE0402925D0 (en) | Novel Compounds | |
CY1108584T1 (en) | 4-PHENYL-5-OXO-1,4,5,6,7,8-HEXAHYDROQUINOLINE DERIVATIVES AS MEDICINES FOR TREATMENT OF STRUCTURE |